依托咪酯
瑞芬太尼
医学
麻醉剂
麻醉学
药品
苯二氮卓
重症监护医学
药物开发
麻醉
三唑仑
药理学
异丙酚
内科学
受体
作者
Nathaniel M. Birgenheier,Ami Stuart,Talmage D. Egan
出处
期刊:Current Opinion in Anesthesiology
[Ovid Technologies (Wolters Kluwer)]
日期:2020-06-08
卷期号:33 (4): 499-505
被引量:26
标识
DOI:10.1097/aco.0000000000000879
摘要
Purpose of review The unique demands of modern anesthesia practice require that medications be effective, well tolerated, and efficient. These attributes are increasingly achieved with the soft drug approach, wherein novel active compounds are specifically designed to be susceptible to rapid biotransformation to inactive metabolites. The present review summarizes the historical background and recent trends in soft drug development in anesthesiology. Recent findings Soft drug development programs for propranadid, etomidate, and benzodiazepine analogues have been undertaken in recent years. Although all three drugs advanced into human trials, neuro-excitatory adverse effects hampered the propranadid and etomidate analogue projects. Remimazolam, the soft benzodiazepine analogue, is at an advanced stage of development, having already received regulatory approval or review in several countries. Summary With succinylcholine as the historical forerunner and remifentanil as the modern prototype, the soft drug paradigm continues to hold promise for the future of anesthesia drug development.
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